Radiochemist

Eckert & Ziegler RadioPharma Inc; Wilmington (MA); Sur place; USD 80 000 - 120 000; Plein temps

Avantages offerts par ce poste

Health insurance

Disability coverage

Life insurance

401(k) plan with company match

Paid time off

Résumé du poste

Eckert & Ziegler Radiopharma, Inc. in Wilmington, MA is seeking a Radiochemist to support isotope production and radiolabeling activities in a cGMP environment. The role requires direct radiolabeling experience and a chemistry degree with hands-on radiochemistry exposure.

On-site, full-time work with daily lab operations and cross-functional collaboration are essential. Responsibilities include process validation, technical transfers, and compliance with USP <825> and 21 CFR Part 211,

Qualifications

• Direct radiolabeling experience is required.
• Bachelor’s degree in Chemistry with 1–3 years radiochemistry experience, or Master’s with at least 1 year radiochemistry experience.
• Experience with PET IND radiochemistry is preferred.
• Strong working knowledge of USP <825> and cGMP requirements under 21 CFR Part 211.
• Proficiency with hot-cell manipulators and standard radiochemistry equipment.
• Demonstrated experience in a cGMP radiochemistry production environment.
• Strong troubleshooting, organizational, and communication skills.
• Ability to work full-time on-site in Wilmington, MA.

Responsabilités

• Support Y-90 and Lu-177 isotope production activities.
• Support radiolabeling campaigns for client projects.
• Participate in technical transfer and process validation activities for new projects.
• Assist with evaluating proposals and provide input to project teams.
• Ensure compliance with USP <825> and 21 CFR Part 211 in daily radiochemistry operations.
• Collaborate with QA, QC, vendors, and project management to support readiness and timely execution.
• Maintain isotope production documentation and cGMP records.
• Handle and manage radioactive waste safely per safety procedures.

Connaissances

Direct radiolabeling experience

PET IND radiosynthesis

USP <825> knowledge

cGMP knowledge

Radiochemistry production experience

Troubleshooting

Organizational skills

Communication skills

Cross-functional collaboration

On-site work

Formation

Bachelor's degree in Chemistry

Master's degree in Chemistry

Outils

Hot-cell manipulators

Radiochemistry equipment

Description du poste

If you are unable to complete this application due to a disability, contact this employer to ask for an accommodation or an alternative application process.

Production Full Time Wilmington, MA, US

19 days ago Requisition ID: 1018

Salary Range: $80,000.00 To $120,000.00 Annually

About Eckert & Ziegler Radiopharma, Inc.

Eckert & Ziegler Radiopharma, Inc. (EZRI) is a U.S.-based subsidiary of Eckert & Ziegler AG, a global leader in isotope technology and radiopharmaceutical manufacturing.

Our mission is to help biotechnology and pharmaceutical partners accelerate radiopharmaceutical innovation while maintaining the highest standards of safety, quality, and current Good Manufacturing Practice (cGMP) compliance.

EZRI operates a clinical-stage manufacturing site in Wilmington, Massachusetts, supporting:

• Yttrium-90 (Y-90) production
• Lutetium-177 (Lu-177) production
• Contract manufacturing services for radiolabeled pharmaceuticals

Position Summary

EZRI is seeking a Radiochemist to join our team in Wilmington, Massachusetts. This hands-on role supports isotope production and radiolabeling activities within our cGMP operations.

The Radiochemist will work in cGMP radiochemistry laboratories to support isotope production, execute client projects, assist with technical transfers, and contribute to process validation activities.

Key Responsibilities

• Support Y-90 and Lu-177 isotope production activities.
• Support radiolabeling campaigns for client projects.
• Participate in technical transfer and process validation activities for new projects.
• Assist with evaluating the technical feasibility of proposals and provide input to project teams.
• Apply USP <825> and 21 CFR Part 211 requirements in daily radiochemistry operations.
• Collaborate with Quality Assurance, Quality Control, vendors, and project management to support operational readiness and timely execution.
• Prepare, maintain, and execute isotope production documentation.
• Maintain accurate cGMP documentation, including batch records, reports, and change controls.
• Handle and manage radioactive waste safely and in accordance with radiation safety procedures.

Key Performance Expectations

• Support validation and production runs that meet established quality specifications.
• Collaborate effectively with Operations, Quality Assurance, Quality Control, and project teams to achieve production timelines.
• Consistently comply with cGMP, USP <825>, and radiation safety requirements.

Required Qualifications and Skills

• Direct radiolabeling experience is required.
• Bachelor’s degree in Chemistry with one to three years of hands-on radiochemistry experience, or a master’s degree in Chemistry with at least one year of hands-on radiochemistry experience.
• Experience with PET IND radiosynthesis is preferred.
• Strong working knowledge of USP <825> and cGMP requirements under 21 CFR Part 211.
• Proficiency with hot-cell manipulators and standard radiochemistry equipment.
• Demonstrated experience working in a cGMP radiochemistry production environment.
• Strong troubleshooting, organizational, and communication skills.
• Ability to work effectively across functions and adapt to changing project and production needs.
• Ability to work full-time on-site in Wilmington, Massachusetts.

Schedule and Work Environment

• Full-time, on-site position in Wilmington, Massachusetts. Candidates must live within commuting distance.
• Regular weekday, day-shift schedule, with flexibility to support time-sensitive isotope production, order fulfillment, and shipment deadlines.
• Occasional after-hours support may be required for critical business needs.
• Regular coordination with international colleagues, including teams in Germany, across multiple time zones.
• Work is performed primarily in laboratory and production environments, with some office-based responsibilities.
• Must be able to stand or sit for extended periods and perform the routine physical demands of radiochemistry work.
• Must be able to climb stairs to access office and production-support areas.
• Must be able to lift up to 50 pounds.

Compensation

The anticipated salary range for this position is $80,000 to $120,000 per year, plus a 10% annual bonus target.

This range represents a good-faith estimate of the annual compensation that Eckert & Ziegler Radiopharma, Inc. reasonably expects to pay at the time of posting. Final compensation will be determined based on the candidate’s experience and qualifications, including education, relevant skills, internal equity, and the requirements of the role.

The current standard benefits package includes:

• 15 days of paid time off, with one additional day added each year
• Medical, dental, and vision coverage
• Short-term and long-term disability coverage
• Life insurance
• 401(k) plan with Company match

EZRI currently pays 100% of the employee-only medical insurance premium. Coverage for a spouse or partner and eligible dependents is available at the applicable employee contribution rates.

Complete details regarding benefit programs and employee responsibilities are provided in the Employee Handbook. EZRI reserves the right to modify its benefit plans at any time.

Equal Opportunity Employer

Eckert & Ziegler Radiopharma, Inc. is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, genetic information, protected veteran status, or any other characteristic protected by federal, state, or local law.

Notice to Recruiters and Staffing Agencies

EZRI does not accept unsolicited résumés or candidate submissions from recruiters, search firms, or staffing agencies. Any résumé or candidate information submitted to an EZRI employee, by any means, without a valid written agreement for this specific position executed in advance by an authorized EZRI representative will be considered unsolicited.

EZRI will not be responsible for, and will not pay, any fee, commission, or other compensation associated with an unsolicited submission, including if the candidate is subsequently hired.